Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS
Antithrombin Activity
Francisella Tularensis Antibody, IgG
Biopsy, Thymus
11-Deoxycorticosterone, Quantitative, Serum
Glucose, Cerebrospinal Fluid (CSF)
Mitochondrial M2 Antibody, IgG
Nocardiosis
Tropheryma whipplei, Molecular
Magnesium, Serum
LDS
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Multiple Sulfatase Deficiency, Gene Mutation Analysis
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
Multiple Sulfatase Deficiency, Gene Mutation Analysis
Medical Test
Interpretation
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Multiple Sulfatase Deficiency, Gene Mutation Analysis
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